Resuscitator, pulmonary, manual, single use
Access comprehensive regulatory information for Resuscitator, pulmonary, manual, single use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Laerdal Pty Ltd, manufactured by Laerdal Medical AS in Norway. The device registration started on December 14, 2018.
This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.
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TGA ARTG Official Data
Class IIa
Class IIa
Resuscitator, pulmonary, manual, single use
Australia TGA ARTG Registered Device
Good Name: Laerdal Pty Ltd - Resuscitator, pulmonary, manual, single use
Intended Purpose
To manually ventilate an infant, adult or child.
Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
December 14, 2018
Effective Date
December 14, 2018
Sponsor
Name
Laerdal Pty LtdManufacturer